clopidogrel
DrugClopidogrel 75mg once a day plus placebo of cilostazol twice a day
Other names: Plavix, produced by Sanofi-Aventis.
NCT Number: NCT00130039
This study will recruit 480 acute stroke patients with symptomatic intracranial stenosis (M1 segment of Middle cerebral artery (MCA) or basilar artery).
They will be randomly assigned into cilostazol group or clopidogrel group. Every patients will take 100mg of aspirin a day additionally.
The primary outcome variable of this study is Progression rate of symptomatic intracranial stenosis on magnetic resonance angiogram (MRA).
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Notify Me35 year and older
All sexes
Interventional
Phase 4
Prince of Wales Hospital, Hong Kong
[Goal] To Reveal the Effect and Safety of Cilostazol Compared with Clopidogrel on the Prevention of the Progression of Symptomatic Intracranial Arterial Stenosis.
[Trial Design] Double-Blind, Active-Controlled, Randomized, Multicenter Trial
[Participants] Acute ischemic stroke patients with symptomatic intracranial arterial stenosis
[Methods]
Cilostazol 200mg (100mg twice per day) versus clopidogrel 75mg
[Outcome Variables]
Primary Outcome Variable:
Secondary outcome variables:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Clopidogrel 75mg once a day plus placebo of cilostazol twice a day
Other names: Plavix, produced by Sanofi-Aventis.
Cilostazol 100mg twice a day plus placebo of clopidogrel once a day
Other names: cilostazol produced by Korea Otsuka Pharmaceutical
Time frame: 7 months after treatment
Blind reviewers classified the presence and severity of stenosis on middle cerebral arteries and basilar artery on magnetic resonance angiogram (MRA) into 5 grades; normal, mild, moderate, severe and occlusion. Progression was defined as worsening of stenosis by 1 or more grades on final MRA as compared with the baseline MRA.
The progression of symptomatic stenosis is defined as 1 or more grade worsening of the stenosis on the symptomatic artery on MRA.
Time frame: 7 months after treatment
number of patients with new ischemic lesions on FLAIR (Fluid attenuation inversion recovery) images of follow-up MRI, which were determined by slice to slice comparison with baseline MRI.
Time frame: upto 7 months after randomization
including nonfatal ischemic stroke, nonfatal hemorrhagic stroke and fatal stroke
Time frame: upto 7 months after randomization
including nonfatal stroke, nonfatal myocardial infarction and vascular death.
Time frame: upto 7 months after randomization
ischemic stroke event which occured in the vascular territory of initial symptomatic stenosis
Time frame: upto 7 months after randomization
life-threatening or fatal bleeding was defined as any fatal bleeding event, a drop in hemoglobin of ≥ 50g/L, or significant hypotension with need for inotropic agents, symptomatic intracranial hemorrhage, or transfusion of ≥ 4 units of red-blood cells or equivalent amount of whole blood. Major bleeding was defined as significantly disabling bleedings, intraocular bleeding leading to significant visual loss, or bleeding requiring transfusion of ≤ 3 units of red-blood cells or equivalent amount of whole blood
Asan Medical Center
Other
Trial for Efficacy and Safety of Cilostazol on the Progression of Symptomatic Intracranial Stenosis Comparing Clopidogrel
Acronym: TOSS-2
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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